CN103717535A - Metal oxide particles containing titanium oxide coated with silicon dioxide-tin(iv) oxide complex oxide - Google Patents

Metal oxide particles containing titanium oxide coated with silicon dioxide-tin(iv) oxide complex oxide Download PDF

Info

Publication number
CN103717535A
CN103717535A CN201280037509.2A CN201280037509A CN103717535A CN 103717535 A CN103717535 A CN 103717535A CN 201280037509 A CN201280037509 A CN 201280037509A CN 103717535 A CN103717535 A CN 103717535A
Authority
CN
China
Prior art keywords
dioxide
coating
particle
titanium dioxide
metal oxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201280037509.2A
Other languages
Chinese (zh)
Other versions
CN103717535B (en
Inventor
小山欣也
古川智规
浅田根子
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp
Publication of CN103717535A publication Critical patent/CN103717535A/en
Application granted granted Critical
Publication of CN103717535B publication Critical patent/CN103717535B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/61—Additives non-macromolecular inorganic
    • C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00—Compounds of titanium
    • C01G23/04—Oxides; Hydroxides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00—Compounds of titanium
    • C01G23/04—Oxides; Hydroxides
    • C01G23/047—Titanium dioxide
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0838—Manufacture of polymers in the presence of non-reactive compounds
    • C08G18/0842—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents
    • C08G18/0861—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers
    • C08G18/0866—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers the dispersing or dispersed phase being an aqueous medium
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36—Compounds of titanium
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36—Compounds of titanium
    • C09C1/3607—Titanium dioxide
    • C09C1/3653—Treatment with inorganic compounds
    • C09C1/3661—Coating
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/66—Additives characterised by particle size
    • C09D7/67—Particle size smaller than 100 nm
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00—Compounds of titanium
    • C01G23/04—Oxides; Hydroxides
    • C01G23/047—Titanium dioxide
    • C01G23/053—Producing by wet processes, e.g. hydrolysing titanium salts
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C01P2004/82—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases
    • C01P2004/84—Particles consisting of a mixture of two or more inorganic phases two phases having the same anion, e.g. both oxidic phases one phase coated with the other
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31652—Of asbestos
    • Y10T428/31663—As siloxane, silicone or silane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Nanotechnology (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Health & Medical Sciences (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Composite Materials (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)
  • Surface Treatment Of Optical Elements (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

There is provided as metal oxide particles having a high refractive index, and having a microscopic particle diameter in order to ensure high transparency, and almost suppressing excitation caused by ultraviolet rays, a metal oxide particle containing titanium oxide coated with silicon dioxide-stannic oxide complex oxide comprising: a titanium oxide-containing core particle (A); and a coating layer with which the titanium oxide-containing core particle (A) is coated and that is made of silicon dioxide-stannic oxide complex oxide colloidal particles (B) having a mass ratio of silicon dioxide/stannic oxide of 0.1 to 5.0, wherein one or more intermediate thin film layers that are made of any one of an oxide; a complex oxide of at least one element selected from the group consisting of Si, Al, Sn, Zr, Zn, Sb, Nb, Ta, and W; and a mixture of the oxide and the complex oxide are interposed between the titanium oxide-containing core particle (A) and the coating layer made of the silicon dioxide-stannic oxide complex oxide colloidal particles (B).

Description

The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide
Technical field
The present invention relates to a kind of metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide, the dispersion colloidal sol of the mixed solvent of the water of this particle, organic solvent or water and organic solvent, the transparent coating formation coating fluid that contains this particle, and the base material that adheres to transparent coating that uses this coating fluid to form, the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide, there is the nuclear particle (A) that contains titanium dioxide and by the coating of this nuclear particle (A) coating, the mass ratio that above-mentioned coating comprises silicon-dioxide/tindioxide is silicon-dioxide-tindioxide composite oxides colloidal particles (B) of 0.1～5.0, and 1 layer of above intermediate thin rete forms between the above-mentioned nuclear particle that contains titanium dioxide (A) and the above-mentioned coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), above-mentioned intermediate thin rete comprises and is selected from Si, Al, Sn, Zr, Zn, Sb, Nb, the oxide compound of at least a kind of element in Ta and W, composite oxides, or any a kind of the mixture of this oxide compound and these composite oxides.
Background technology
Plastic former, although bring into play the advantage of lightweight, workability, shock-resistance etc. and used in a large number, but contrary, because not and easily damage of hardness, easily by inadequate etc. the reason of nip, charged sorption dust, thermotolerance, when using as glasses lens, window material etc., deposit shortcoming in practical.Therefore, propose plastics forming body to apply the scheme of protection tunicle.The tunicle formation coating fluid that protection tunicle is used is to have proposed kinds of schemes really.
As the scheme giving close to the hard tunicle of inorganic system, take the tunicle formation coating fluid that silicoorganic compound or its hydrolyzate be principal constituent (resinous principle or the forming component of filming), as glasses lens purposes, used (with reference to patent documentation 1).
Above-mentioned tunicle formation coating fluid, also because scuff resistance is not adequate, further proposes its interpolation to be dispersed into the scheme of the silicon dioxide gel of colloidal, practical as glasses lens purposes.(with reference to patent documentation 2).
But plastics glasses lens in the past, most by manufacturing Diethylene Glycol diallylcarbonate monomer injection moulding polymerization.This eyeglass, specific refractory power is about 1.50, lower than the specific refractory power of glass mirror approximately 1.52, the situation in myopia with eyeglass, the shortcoming of marginate thickness thickening.Therefore, the exploitation of the monomer that refractive index ratio Diethylene Glycol diallyl carbonic ether is high is in recent years advancing, and has proposed the scheme (with reference to patent documentation 3 and 4) of high refractive index resins material of the scope of specific refractory power 1.54～1.76.
For such high refractivity resin lens, also once proposed the aqueous colloidal dispersion of metal oxide microparticle of Sb, Ti for the method for coating material (with reference to patent documentation 5 and 6.）。
In addition, a kind of application composition that comprises silane coupling agent and stable modified metal-oxide colloidal sol is disclosed, this modified metal-oxide colloidal sol contains particle (c), and the primary particle size with 2～100nm, this particle (c) be the colloidal particle (a) of metal oxide with the primary particle size of 2～60nm be core, its surface is obtained with serving (b) coating of the colloidal particle that comprises acidic oxide, and (c) is converted into metal oxide with the ratio of 2～50 quality %, contains.And, as the concrete example of the colloidal particle being used, disclose with the modifying titanium dioxide-zirconium dioxide-tindioxide composite gel of the antimony peroxide coating that contains alkylamine etc. (with reference to patent documentation 7.）。In addition, disclose with the titanium dioxide-tindioxide zirconium dioxide composite gel of alkylamine, hydroxycarboxylic acid stabilization etc. (with reference to patent documentation 8.）。
Technical literature formerly
Patent documentation 1: JP 52-11261 communique
Patent documentation 2: JP 53-111336 communique
Patent documentation 3: JP 55-13747 communique
Patent documentation 4: JP 64-54021 communique
Patent documentation 5: JP 62-151801 communique
Patent documentation 6: JP 63-275682 communique
Patent documentation 7: JP 2001-123115 communique
Patent documentation 8: Unexamined Patent 10-306258 communique
Summary of the invention
But, aspect high refractivity resin lens, exist on the tunicle that has used silicon dioxide gel and produce interference fringe, eyeglass outward appearance this problem not attractive in appearance.In addition, used on the tunicle of TiO 2 sol, existed titanium dioxide by ultraviolet ray exited and be coloured to blue problem.In addition, while not applying the situation of antireflection film on this tunicle, cannot suppress the excitation because of UV-induced titanium dioxide, therefore have this problem that easily cracks.
Problem of the present invention, is to provide a kind of metal oxide particle, and it can be adjusted into can be for refractive index n dit is the high refractive index that 1.54～1.76 middle high refractive index plastic basis material is used, and there is the nominal particle size that can guarantee high transparent, substantially suppressed because of UV-induced excitation, in addition, be also to provide the transparent coating that contains such particle to form with coating fluid and the base material that adheres to transparent coating.
The present invention, as its 1st viewpoint, it is a kind of metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide, it has the nuclear particle (A) that contains titanium dioxide and by the coating of this nuclear particle (A) coating, the mass ratio that above-mentioned coating comprises silicon-dioxide/tindioxide is silicon-dioxide-tindioxide composite oxides colloidal particles (B) of 0.1～5.0, and 1 layer of above intermediate thin rete forms between the above-mentioned nuclear particle that contains titanium dioxide (A) and the above-mentioned coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), above-mentioned intermediate thin rete comprises and is selected from Si, Al, Sn, Zr, Zn, Sb, Nb, the oxide compound of at least a kind of element in Ta and W, composite oxides, or any a kind of the mixture of this oxide compound and these composite oxides,
As the 2nd viewpoint, be that the content of titanium dioxide in the above-mentioned nuclear particle that contains titanium dioxide (A) is with TiO according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in the 1st viewpoint 2be scaled 5～100 quality %, the amount of the above-mentioned coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B) is with respect to the quality of the above-mentioned nuclear particle that contains titanium dioxide (A), the scope 0.01～1.0;
As the 3rd viewpoint, according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in the 1st viewpoint or the 2nd viewpoint, the above-mentioned nuclear particle that contains titanium dioxide (A), for comprising the nuclear particle that is selected from least a kind of element in Si, Al, Sn, Zr, Zn, Sb, Nb, Ta and W;
As the 4th viewpoint, be that the crystal formation of the above-mentioned nuclear particle that contains titanium dioxide (A) is rutile-type according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of the 1st viewpoint～3rd viewpoint;
As the 5th viewpoint, be according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of the 1st viewpoint～4th viewpoint, in surface bonding, there are silicoorganic compound or amine compound;
As the 6th viewpoint, that a kind of metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide disperses colloidal sol, that the metal oxide particle that metal oxide particle is scattered in dispersion medium disperses colloidal sol, above-mentioned metal oxide particle is the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of the 1st viewpoint～5th viewpoint, and above-mentioned dispersion medium is the mixed solvent of water, organic solvent or water and organic solvent;
As the 7th viewpoint, it is a kind of transparent coating formation coating fluid, comprise metal oxide particle and matrix forming component, the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one that above-mentioned metal oxide particle contains the 1st viewpoint～5th viewpoint, above-mentioned matrix forming component contains at least a kind that is selected from silicoorganic compound, the hydrolyzate of these silicoorganic compound and the partial condensate of this hydrolyzate representing with following formula I
R 1 aR 2 bSi（OR 3） 4-（a+b） （Ⅰ）
(in formula, R 1represent alkyl, vinyl, the methacryloxy of carbonatoms 1～10 or there is the organic group of sulfydryl, amino or epoxy group(ing), R 2the alkyl that represents carbonatoms 1～4, R 3the alkyl or the acyl group that represent carbonatoms 1～8, a, b represent 0 or 1);
As the 8th viewpoint, it is a kind of transparent coating formation coating fluid, comprise metal oxide particle and matrix forming component, the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one that above-mentioned metal oxide particle contains the 1st viewpoint～5th viewpoint, above-mentioned matrix forming component contains at least a kind of resin being selected from heat-curing resin, thermoplastic resin and uv curing resin;
As the 9th viewpoint, be according to the transparent coating formation coating fluid described in the 8th viewpoint, above-mentioned matrix forming component is that polyester based resin or ammonia ester are resin;
As the 10th viewpoint, be a kind of base material that adheres to transparent coating, the transparent coating having on surface described in any one of the 7th viewpoint～9th viewpoint forms the transparent coating forming with coating fluid;
As the 11st viewpoint, it is a kind of base material that adheres to transparent coating, on surface, there is the transparent coating using described in the 8th viewpoint or the 9th viewpoint and form the bottom coating forming with coating fluid, and further there is the transparent coating using described in the 7th viewpoint thereon and form the hard coat film forming with coating fluid;
As the 12nd viewpoint, be according to the base material that adheres to transparent coating described in the 10th viewpoint or the 11st viewpoint, on above-mentioned transparent coating or hard coat film, further there is antireflection film.
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention, it has the nuclear particle (A) that contains titanium dioxide and by the coating of this nuclear particle (A) coating, the mass ratio that above-mentioned coating comprises silicon-dioxide/tindioxide is silicon-dioxide-tindioxide composite oxides colloidal particles (B) of 0.1～5.0, and 1 layer of above intermediate thin rete forms between the above-mentioned nuclear particle that contains titanium dioxide (A) and the above-mentioned coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), above-mentioned intermediate thin rete comprises and is selected from Si, Al, Sn, Zr, Zn, Sb, Nb, the oxide compound of at least a kind of element in Ta and W, composite oxides, or any a kind of the mixture of this oxide compound and these composite oxides, the transparent coating being engaged on the base material that transparent coating is formed to synthetic resin lens etc. when this metal oxide particle forms with in the situation of coating fluid, even by uviolizing on this transparent coating, the also nondiscoloration or fade of this transparent coating.That is, metal oxide particle of the present invention, is the metal oxide particle of weathering resistance, excellent in light-resistance.
In addition, metal oxide particle of the present invention, so have a high transparent because particle diameter is small.
In addition, according to the present invention, by the mass ratio of metal oxide particle or the composition of the metal oxide particle that change contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide that change the matrix forming component in coating fluid and contain silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide, can easily adjust the specific refractory power that is formed at the transparent coating on base material.Therefore, transparent coating formation coating fluid of the present invention, can make the specific refractory power of transparent coating and the specific refractory power of base material that by this coating fluid, form equate, can eliminate resulting from the interference fringe of both refringences, thus can as in the transparent coating used of the eyeglass of high refractive index form and use well with coating fluid.On the other hand, make the specific refractory power of tunicle with respect in the very high situation of the specific refractory power of base material, can make the glossiness of substrate surface very high.
The transparent coating that use the present invention relates to forms and is formed at the tunicle on base material with coating fluid, because titanium dioxide is contained in the metal oxide particle in tunicle as principal constituent, so ultraviolet screening effect is also fine, as the surface coatings of automobile etc., film or its its both very suitable outward.
In addition, it is colourless, transparent with the tunicle that coating fluid is formed on base material that the transparent coating that use the present invention relates to forms, excellent with adaptation, weathering resistance, photostabilization, resistance to chemical reagents, pliability and the dyeability of base material, and surface hardness is high, so scuff resistance and excellent in wear resistance.Therefore, providing the aspects such as the various optical mirror slips of glasses lens, camera etc., various display element spectral filter, mirror (sight glass) very suitable.In addition, if the high refractive index layer when forming multi anti reflection coating on the substrate surface at mirror, window glass and various display element strainers etc. forms the transparent coating formation coating fluid the present invention relates to, content is high-visible.
If form such antireflection film on various display element faces, luminescent lamp etc. can not mirror on these display element faces, so that reflection becomes is distinct, eyes can be tired.
Embodiment
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide of the present invention, it is characterized in that: there is the nuclear particle (A) that contains titanium dioxide and by the coating of this nuclear particle (A) coating, above-mentioned coating comprises silicon-dioxide-tindioxide composite oxides colloidal particle, and 1 layer of above intermediate thin rete forms between the above-mentioned nuclear particle that contains titanium dioxide (A) and the above-mentioned coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), above-mentioned intermediate thin rete comprises and is selected from Si, Al, Sn, Zr, Zn, Sb, Nb, the oxide compound of at least a kind of element in Ta and W, composite oxides, or any a kind of the mixture of this oxide compound and these composite oxides.
Though the primary particle size that contains the metal oxide particle of silicon-dioxide-tindioxide composite oxides coating titanium dioxide above-mentioned is not particularly limited, and is 1～100nm, is preferably the scope of 2～60nm.At this so-called primary particle size, refer to by the particle diameter of transmission electron microscope Observe and measure.
Above-mentioned primary particle size is in the situation lower than 1nm, and it is insufficient by film hardness that the coating fluid that use comprises this particle obtains, and rub resistance and wearability are poor.And, sometimes can not fully improve the specific refractory power of tunicle.In addition, when primary particle size surpasses 100nm, can become gonorrhoea and opaque of the tunicle sometimes obtaining.
The primary particle size of the above-mentioned nuclear particle that contains titanium dioxide (A), though be not particularly limited, expectation is roughly 1～100nm, is preferably the scope of 2～50nm.
Content of titanium dioxide in the above-mentioned nuclear particle that contains titanium dioxide (A), by TiO 2be scaled 5～100 quality %, preferably more than 10 quality %, more preferably more than 20 quality %.Content of titanium dioxide is lower than in 10% situation, and the specific refractory power of the transparent coating that the coating fluid that use contains these particles obtains does not uprise, and according to the specific refractory power of base material, produces sometimes interference fringe.
The above-mentioned nuclear particle that contains titanium dioxide (A), can only consist of titanium dioxide, also can comprise titanium dioxide and titanium dioxide composition in addition.The above-mentioned nuclear particle that contains titanium dioxide (A), preferably comprises at least a kind of element being selected from Si, Al, Sn, Zr, Zn, Sb, Nb, Ta and W.Composition beyond such titanium dioxide and titanium dioxide, can be mixture, can be also mutually solid solution condition.
As the concrete example that contains the situation of titanium dioxide composition in addition in the above-mentioned nuclear particle that contains titanium dioxide (A), can enumerate the particle that comprises titanium dioxide and tindioxide or comprise titanium dioxide, tindioxide and zirconium dioxide.
In addition, the above-mentioned nuclear particle that contains titanium dioxide (A) can be amorphous, can be also the crystallization of Detitanium-ore-type, rutile-type, brookite etc.In addition can also be that barium titanate (is used BaTiO, 3or BaOTiO 2represent) such perovskite typed titanium compound.Wherein, the crystal formation of the above-mentioned nuclear particle that contains titanium dioxide (A) is preferably rutile-type.
The amount of the coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B) in the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide of the present invention, the scope that is 0.01～1.0 with respect to the above-mentioned nuclear particle that contains titanium dioxide (A).
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide of the present invention, 1 layer of above intermediate thin rete between the nuclear particle that contains titanium dioxide (A) and the coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), any a kind of the mixture that above-mentioned intermediate thin rete comprises the oxide compound, composite oxides or this oxide compound and these composite oxides that are selected from least a kind of element in Si, Al, Sn, Zr, Zn, Sb, Nb, Ta and W.This intermediate thin rete can be 1 layer, can be also 2 layers of above multilayer.
By intermediate thin rete, between the coating that contains the nuclear particle of titanium dioxide (A) and comprise silicon-dioxide-tindioxide composite oxides colloidal particles (B), at least there is 1 layer, the specific refractory power that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide metal oxide particle can be adjusted, many physical property of the adaptation etc. of the photostabilization, weathering resistance, tunicle and the base material that use the tunicle that the coating fluid contain this particle obtains can be improved in addition.In addition, can suppress the painted of the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide, improve the transparency of tunicle.
In addition, the ratio of the nuclear particle that contains titanium dioxide (A) in the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide and the coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), the quality of the above-mentioned nuclear particle that contains titanium dioxide (A) of take is benchmark, amount as the coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), the words of the scope in 0.01～1.0, at least arrange 1 layer intermediate thin rete layer quantity, layer thickness be not particularly limited.
As above-mentioned intermediate thin rete, preferred silicon-dioxide especially, weisspiessglanz, aluminum oxide or zirconium white, as form, it can be each composition stratification thin film layer of silicon-dioxide, weisspiessglanz, aluminum oxide or zirconium white, or, can be also for example weisspiessglanz-silica complex like that Composite form thin film layer.
In this situation, as intermediate thin rete, use silicon oxide and zirconium white and/or aluminum oxide, can obtain forming there is excellent weather resistance, photostabilization, and the adaptation of base material, film hardness, scuff resistance, pliability etc. transparent coating contain sb oxide coating titania composite oxide particle.In addition, because thin film layer contains silicon oxide, composite oxides are the stability raising of particle disperse water colloidal sol thus, and the useful life of aftermentioned coating fluid is elongated, the hardness of the transparent coating that can seek to obtain improve and with the raising of the adaptation of the antireflection film forming on transparent coating, this situation also improves weathering resistance, photostabilization, the adaptation with base material, film hardness, scuff resistance, pliability etc. in addition.
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention, preferably has silicoorganic compound or amine compound in its surface bonding.
Silicoorganic compound as using, can be used as the well-known silicoorganic compound of silane coupling agent, and its kind, according to suitably selections such as the kinds of purposes and solvent.
As silicoorganic compound, particularly, use the compound being represented by following general formula (1)～(4).
With general formula (1): R 3siX (1)
The simple function silane representing (in formula (1), R represent carbonatoms 1～8 alkyl, phenyl, vinyl, methacryloxy, there is the organic group of sulfydryl, amino or epoxy group(ing).X represents hydrolization group).As such simple function silane, for example can enumerate trimethyl silane, dimethylphenylsilaneand, dimethyl vinyl silanes etc.
With general formula (2): R 2siX 2(2)
The difunctionality silane representing (in formula (2), R represent carbonatoms 1～8 alkyl, phenyl, vinyl, methacryloxy, there is the organic group of sulfydryl, amino or epoxy group(ing).X represents hydrolization group).As such difunctionality silane, for example can enumerate dimethylsilane, diphenyl silane etc.
With general formula (3): RSiX 3(3)
The trifunctional silane representing (in formula (3), R represent carbonatoms 1～10 alkyl, phenyl, vinyl, methacryloxy, there is the organic group of sulfydryl, amino or epoxy group(ing).X represents hydrolization group).As such trifunctional silane, for example can enumerate methyl-monosilane, phenyl silane etc.
With general formula (4): SiX 4(4)
Four functional silanes (in formula (4), X represents hydrolization group) that represent.As four such functional silanes, for example can enumerate the tetraalkoxysilane of tetraethoxysilane etc. etc.
These silicoorganic compound, may be used alone, can also be two or more kinds in combination.In addition, can be when making silicoorganic compound be incorporated into the above-mentioned surperficial surfaction that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle to process, carry out the partial hydrolysis of above-mentioned silicoorganic compound, under the state that also can not be hydrolyzed, carry out surfaction processing.In addition, after surfaction is processed, the surperficial hydroxyl reaction of selective hydrolysis group and the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide state, but a part of hydroxyl keeps untreated and remaining state also harmless.
In addition, as the amine compound using, there is the alkylamine of ethamine, triethylamine, Isopropylamine, Tri N-Propyl Amine etc., the aryl amine of benzyl amine etc., the aliphatic cyclic amine of piperidines etc., the alkanolamine of monoethanolamine, trolamine etc., the quaternary ammonium salt of Tetramethylammonium hydroxide etc. or quaternary ammonium hydroxide.
These amine compounds, can be used separately also and can two or more mix use.
In addition, these amine compounds, for example, also can be by the hydroxyl reaction with the above-mentioned metal oxide particle surface of containing silicon-dioxide-tindioxide composite oxides coating titanium dioxide, or by this particle surface coordination combination, make it in the surface bonding of this particle.
Make the metal oxide particle surface bonding that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide have silicoorganic compound or amine compound, for example, can in the alcoholic solution of silicoorganic compound or amine compound, mix the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide, add the water of specified amount and add as required after hydrolyst, place at normal temperatures with the specified time, or carry out heat treated.
In addition, also can be by adding the mixed solution heat treated of water and alcohol to carry out the hydrolyzate of silicoorganic compound and the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide.
The silicoorganic compound that use or the amount of amine compound, can, with respect to the metal oxide particle quality of the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide, add 0.1～40 quality %.
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention, the metal oxide can be used as in the mixed solvent that is scattered in water, organic solvent or water and organic solvent disperses colloidal sol to process
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention disperses colloidal sol, is the colloidal sol that the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide is scattered in the mixed solvent of water, organic solvent or water and organic solvent.
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention disperses colloidal sol, because be provided with above-mentioned intermediate thin rete, so compare the excellences such as dispersion stabilization with the composite oxide sol of known TiO 2 sol, TiO 2 series in the past.
Total metal oxide concentration in the water-dispersion colloidal sol of the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides colloidal particle coating titanium dioxide is 0.01～40 quality %, be preferably the scope of 0.5～20 quality %.In the situation of total metal oxide concentration lower than 0.01 quality %, the concentration of the coating fluid sometimes obtaining with other components matching becomes too low, and the thickness of filming obtaining cannot reach desirable thickness.Total metal oxide concentration surpasses 40 quality %, and the stability of colloidal sol can become insufficient sometimes.
The complex metal oxides particle organic solvent that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide disperses the situation of colloidal sol, preferably the surface bonding at the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide has silicoorganic compound or amine compound, carries out surfaction processing.Colloidal sol after surfaction is processed, since surface-hydrophobicized, so the excellent dispersion to organic solvent.
The organic solvent of the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide disperses the total metal oxide concentration in colloidal sol, is 1～60 quality %, the preferably scope of 2～30 quality %.In the situation of total metal oxide concentration lower than 1 quality %, the concentration of coating fluid sometimes obtaining with other components matching etc. becomes too low, and the thickness of filming obtaining cannot reach desirable thickness.Solid component concentration surpasses 60 quality %, and collosol stability can become insufficient.
Organic solvent as the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention disperses the organic solvent using in colloidal sol, can enumerate methyl alcohol particularly, ethanol, the alcohols of Virahol etc., methylcyclohexane, the cellosolve class of ethyl cellosolve etc., the glycols of ethylene glycol etc., ritalin, the lipid of vinyl acetic monomer etc., diethyl ether, the ethers of tetrahydrofuran (THF) etc., acetone, the ketone of methyl ethyl ketone etc., the halogenated hydrocarbons of ethylene dichloride etc., toluene, dimethylbenzene etc. aromatic hydrocarbon based, and N, dinethylformamide etc.These solvents also can two or more mix use.
The the first transparent coating formation coating fluid the present invention relates to, it is characterized in that, in silicoorganic compound, the hydrolyzate of silicoorganic compound or the partial condensate of this hydrolyzate that comprises the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide and represent as the following logical formula I of use of matrix forming component more than a kind
R 1 aR 2 bSi（OR 3） 4-（a+b） （Ⅰ）
(in formula, R 1represent alkyl, vinyl, the methacryloxy of carbonatoms 1～10 or there is the organic group of sulfydryl, amino or epoxy group(ing), R 2the alkyl that represents carbonatoms 1～4, R 3the alkyl or the acyl group that represent carbonatoms 1～8, a, b represent 0 or 1).
As the silicoorganic compound that represent with above-mentioned general formula (I), can enumerate tetramethoxy-silicane particularly, tetraethoxysilane, methyltrimethoxy silane, ethyl triethoxysilane, Union carbide A-162, phenyl triethoxysilane, dimethyldimethoxysil,ne, phenyl methyl dimethoxy silane, vinyltrimethoxy silane, vinyltriethoxysilane, vinyl three (β-trimethylammonium oxyethyl group) silane, γ-glycidyl ether oxygen base propyl trimethoxy silicane ((γ-glycidoxypropyl) trimethoxysilane), γ-glycidyl ether oxygen base propyl-triethoxysilicane, γ-glycidyl ether oxygen base propyl group methyl dimethoxy base silane, γ-glycidyl ether oxygen base propyl group methyl diethylsilane, β-(3,4-epoxy group(ing) cyclohexyl) ethyl trimethoxy silane, γ-methacryloxypropyl trimethoxy silane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, N-(β-aminoethyl)-γ-aminopropyl methyl dimethoxysilane, γ-aminopropyl triethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, γ-mercaptopropyl trimethoxysilane etc.They can use separately also can two or more mix use.
In addition, these silicoorganic compound, preferably, in the polar organic solvent of solvent-free lower or alcohol etc., under sour existence, hydrolysis is used.
The mixing of the silicoorganic compound that represent with above-mentioned general formula (I) and the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide, can, after the hydrolysis of the silicoorganic compound that represent with above-mentioned general formula (I), also can after the complex metal oxides mix particles with containing silicon-dioxide-tindioxide composite oxides coating titanium dioxide, be hydrolyzed.Hydrolysis can be complete hydrolysis, can be also that its part is partly hydrolyzed.
Moreover it is 10～90 quality % by the ratio of occupying in coating fluid that above-mentioned matrix forming component forms at transparent coating, the scope that is preferably made as 20～80 quality % is more suitable.This ratio is below 10 quality %, and the adaptation of base material and tunicle reduces sometimes, in addition, more than 90 quality %, sometimes cannot obtain the tunicle of high refractive index.
In addition, the second transparent coating formation coating fluid of the present invention, it is characterized in that, comprise the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide and as at least a kind of resin in heat-curing resin, thermoplastic resin and uv curing resin that is selected from of matrix forming component.
As above-mentioned matrix forming component, can enumerate acrylic resin, melamine series resin, ammonia ester and be resin, vibrin, phosphocreatine (phosphagen) is resin etc.Wherein, preferred polyester is that resin or ammonia ester are resin.
Transparent coating formation coating fluid of the present invention, 110 ℃ of drying solid compositions with respect to 100 mass parts matrix forming components, the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide is 5～1000 mass parts, preferably 10～600 mass parts.
Transparent coating of the present invention forms with in coating fluid, also can optionally comprise following (C)～(F) composition outside the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides titanium dioxide and matrix forming component.
(C) composition:
(C) composition is for using general formula (5): Si(OR 4) 4(5)
(in formula (5), R 4the alkyl, alkoxyalkyl or the acyl group that represent carbonatoms 1～8) hydrolyzate or the more than a kind of partial condensate of the four sense silicoorganic compound that represent.
The silicoorganic compound that represent with above-mentioned general formula (5), for the specific refractory power of adjusting the transparent coating forming, the curing speed of the transparent coating that has further accelerated to be coated with, improve transparent coating hardness object and use.By using (C) composition, can suitably adjust the specific refractory power of the transparent coating after solidifying according to the specific refractory power of base material, even and the content of the complex metal oxides particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide reduces to a certain extent, also can obtain the adaptation of antireflection film.
As the four sense silicoorganic compound that represent with general formula (5), can enumerate particularly tetramethoxy-silicane, tetraethoxysilane, tetrapropoxysilane, tetraisopropoxysilan, four butoxy silanes, tetraphenoxy-silicane alkane, tetrem acyloxy silane, tetraalkoxysilane, four (2-methoxy ethoxy) silane, four (2-ethyl butoxy silane), four (2-ethyl hexyl oxy) silane etc.They can use separately also can two or more mix use.In addition, they are preferably in the organic solvent of solvent-free lower or alcohol etc., and under sour existence, hydrolysis is used.
Moreover, above-mentioned (C) composition transparent coating form with in coating fluid, occupy containing proportional, the transparent coating of take formation is benchmark by the quality of coating fluid, is preferably 0～50 quality %.This is because if containing easily cracking in the proportional transparent coating surpassing after 50 quality % solidify.
(D) composition:
(D) composition is to be selected from metal oxide microparticle of at least a kind of element in Si, Al, Sn, Sb, Ta, Ce, La, Zn, W, Nb, Zr and In or the complex metal oxides of a kind of above element, and primary particle size is 1～50nm.They are in particular SiO 2, Al 2o 3, SnO 2, Sb 2o 5, Ta 2o 5, CeO 2, La 2o 3, ZnO, WO 3, ZrO 2, In 2o 3, Nb 2o 5deng metal oxide microparticle, ZnSbO 6, ZnSnO 3deng composite oxide particle or these both sides with colloidal particle shape, be scattered in the composition of water or organic solvent.
(D) composition, also can be used silicoorganic compound that any same form in the useful above-mentioned general formula of its surface bonding (1)～(4) represents or the composition of amine compound.
(E) composition:
(E) composition is at least one being selected from multi-functional epoxy compounds, polycarboxylic acid and polybasic acid anhydride.The hardness improvement of the transparent coating that forms of take is used as object.
So-called multi-functional epoxy compounds, is the epoxy resin in 1 molecule with 2 above epoxy group(ing), can enumerate in the past known ethylene glycol diglycidylether, Diethylene Glycol diglycidylether, 1,4-cyclohexanedimethanodiglycidyl diglycidyl ether etc.
As polycarboxylic acid and polybasic acid anhydride, can enumerate propanedioic acid, succsinic acid, hexanodioic acid, nonane diacid, toxilic acid, terephthalic acid, terephthalic acid, fumaric acid, methylene-succinic acid, oxaloacetic acid, succinyl oxide, maleic anhydride, itaconic anhydride, 2,3-dimethyl maleic anhydride, anhydride phthalic acid etc.
(E) composition transparent coating form with in coating fluid, occupy containing proportional, the transparent coating of take formation is benchmark by the quality of coating fluid, is preferably 0～40 quality %.This is because surpass 40 quality %, and the transparent coating after solidifying reduces with the adaptation of the antireflection film forming on it.
(F) composition:
(F) composition, for being selected from the curing catalysts of at least a kind in salt, acids and the metal chloride of amine, amino acids, cetylacetone metallic, metal salts of organic acids, perchloric acid class, perchloric acid class.(F) composition is that silanol group or the solidifying of epoxy group(ing) that the silicon-type matrix forming component for promoting transparent coating formation to comprise with coating fluid has used.By using these curing catalysts, can accelerate tunicle and form reaction.
As their concrete example, can enumerate the amine of n-Butyl Amine 99, triethylamine, guanidine, biguanides etc., the amino acids of glycine etc., the cetylacetone metallic of aluminium acetylacetonate, chromium acetylacetonate, titanium acetylacetone, acetylacetone cobalt etc., the organic acid metal salt of sodium-acetate, zinc naphthenate, cobalt naphthenate, zinc octoate, stannous octoate etc., acid or the SnCl of the perchloric acid class of perchloric acid, ammoniumper chlorate, magnesium perchlorate etc. or its salt, hydrochloric acid, phosphoric acid, nitric acid, p-toluenesulphonic acids etc. 2, AlCl 3, FeCl 3, TiCl 4, ZnCl 2, SbCl 3deng lewis acidic metal chloride etc.
These curing catalysts, can form and use by the adjustment kinds such as composition and the usage quantity of coating fluid according to transparent coating.As the upper limit of usage quantity, wish to be that 5 quality % are used below by the total solids composition with respect in above-mentioned coating fluid.
In addition, for improvement, use transparent coating of the present invention and form the performance that is formed at the transparent coating on base material with coating fluid, as required, also can add a small amount of tensio-active agent, charged preventor, UV light absorber, oxidation inhibitor, dispersed dye, oil-soluble dyes, fluorescence dye, pigment, photochromic compound, thixotropic agent etc.
To transparent coating formation coating fluid of the present invention, for the object of giving mobility, adjustment solid component concentration, adjustment sheet surface tension, viscosity, velocity of evaporation etc., can use solvent.The solvent using is water or organic solvent.
As the organic solvent using, can enumerate the alcohols of methyl alcohol, ethanol, Virahol etc., the cellosolve class of methylcyclohexane, ethyl cellosolve etc., the glycols of ethylene glycol etc., the lipid of ritalin, vinyl acetic monomer etc., the ethers of diethyl ether, tetrahydrofuran (THF) etc., the ketone of acetone, methyl ethyl ketone etc., the halogenated hydrocarbons of ethylene dichloride etc., toluene, dimethylbenzene etc. aromatic hydrocarbon based, with DMF etc.
Manufacture method as the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention, can adopt known method in the past.
As the nuclear particle that contains titanium dioxide (A), for example, can adopt the manufacture method of the disclosed composite oxide particles such as Japanese kokai publication hei 10-306258 communique of being applied for by the applicant to manufacture.The solid component concentration of the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A) is 0.1～30 quality % as total metal oxide, is preferably the scope of 0.5～20 quality %.In the situation of the concentration of above-mentioned water-dispersion colloidal sol lower than 0.1 quality %, productivity is low, to unfavorable in industrial production.In addition, solid component concentration surpasses 30 quality %, and the particle obtaining has the tendency that becomes agglomeration, because be difficult to obtain excellent transparent coating, so not preferred.
The formation method of the above-mentioned intermediate thin rete of any a kind of the mixture that comprises the oxide compound, composite oxides or this oxide compound and these composite oxides that are selected from least a kind of element in Si, Al, Sn, Zr, Zn, Sb, Nb, Ta and W, first, preparation becomes the aqueous solution or the colloidal particle dispersion liquid of element of the constituent of intermediate film layer, the nuclear particle that contains titanium dioxide (A) is dropped into wherein, and the surface of the nuclear particle that contains titanium dioxide at this (A) forms intermediate thin rete.While forming intermediate thin rete, preferably heating, preferably 40～200 ℃.
Then, in the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A) that forms intermediate thin rete, add the water-dispersion colloidal sol of silicon-dioxide-tindioxide composite oxides colloidal particles (B), form coating.The addition of silicon-dioxide-tindioxide composite oxides colloidal particles (B), the scope that is 0.01～1.0 with respect to the above-mentioned nuclear particle that contains titanium dioxide (A).
The water-dispersion colloidal sol of the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide obtaining by above-mentioned method, suitably regulates pH value, the temperature of disperseing colloidal sol as required, also can heat as required.Preferably 40～200 ℃ of heating.After coating forms, also can remove impurity by carrying out washing treatment as required.In addition, can, by the method for ultra-filtration, evaporation concentration etc., adjust total metal oxide concentration.
The metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide of the present invention disperses colloidal sol, is to take the colloidal sol that the mixed solvent of water, organic solvent or water and organic solvent is dispersion medium.Above-mentioned organic solvent disperses colloidal sol, can adopt the normally used method of distillation method or ultra-filtration method etc., and the water of the dispersion medium as above-mentioned dispersion colloidal sol is carried out to solvent exchange and manufactures.
Transparent coating formation coating fluid of the present invention, can be by the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide that adopts aforesaid method to obtain, mixed matrix forming component and other compositions as required and obtain.
Manufacture transparent coating of the present invention and form while using coating fluid, can use well the above-mentioned metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide to disperse colloidal sol.
Above-mentioned transparent coating forms the solid component concentration with coating fluid, comprise come from mix as required other compositions that use solids component in interior total concentration, be 1～70 quality %, be preferably the scope of 2～50 quality %.
Moreover, manufacturing transparent coating of the present invention forms while using coating fluid, using under the form at above-mentioned dispersion colloidal sol, the in the situation that the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide can easily disperseing in coating fluid, also can under the state of micropowder, use, further also can use the dried material of above-mentioned dispersion colloidal sol.
Then, with regard to the base material that adheres to transparent coating of the present invention, describe.The base material that adheres to transparent coating of the present invention, has the transparent coating in base material and the high refractive index that forms at substrate surface, and this transparent coating is formed with coating fluid and formed by above-mentioned transparent coating.
The base material that adheres to transparent coating of the present invention, is characterized in that, at substrate surface, has and uses the above-mentioned first or second transparent coating to form the transparent coating forming with coating fluid.
In addition, the base material that adheres to transparent coating of the present invention, it is characterized in that having and use above-mentioned the second transparent coating to form the bottom coating forming with coating fluid at substrate surface, and further there is the hard coat film that uses the first transparent coating formation to form with coating fluid thereon.On above-mentioned transparent coating or hard coat film, further also can there is antireflection film.
The base material using, can be used the various base materials that comprise glass, plastics etc., can enumerate particularly the light cover that the paint film of the various optical mirror slips of glasses lens, camera etc., various display element spectral filter, mirror, window glass, automobile etc., automobile etc. use.On this substrate surface, as hard coat film, form transparent coating.Or beyond hard coat film, also the bottom coating as glass lens forms transparent coating with film sometimes.
These are formed at the thickness of the tunicle of substrate surface, although according to adhering to the purposes of base material of tunicle and difference, preferably 0.05～30 μ m.
The base material that adheres to transparent coating of the present invention, can be at above-mentioned substrate surface, by transparent coating formation coating fluid of the present invention, adopt the known method coating, dry in the past such as pickling process, method of spin coating, spray method, print roll coating method, flow coat method, form tunicle, the heat resisting temperature that then this tunicle is heated to base material is manufactured below thus.Especially, the eyeglass base material to heat-drawn wire lower than 100 ℃, does not preferably need the method for spin coating with fixture fixing len base material.In addition, in the situation that it is resin lens with base material that tunicle forms, wish on base material, to be coated with after coating fluid, the temperature heat drying a few hours with 40～200 ℃, form thus tunicle.
Moreover, as above-mentioned transparent coating, form the matrix forming component with coating fluid, in the situation that having used uv curing resin, can utilize after substrate surface has been coated with this coating fluid and be dried, thereby the substrate surface being coated with at this coating fluid irradiates the ultraviolet ray of provision wavelengths solidifies the method waiting, and manufactures the base material that adheres to tunicle the present invention relates to.
In addition, while manufacturing the base material that adheres to tunicle of the present invention, for improving base material, for example eyeglass base material, with the object of the adaptation of tunicle, also substrate surface can be processed with alkali, acid or tensio-active agent in advance, with inorganic or organic particle, carry out milled processed, carry out bottoming processing or Cement Composite Treated by Plasma.
In addition, as the base material that adheres to tunicle of the present invention, also can between base material and hard coat film layer, there is bottom coating.In this situation, by bottom coating use above-mentioned second transparent coating form for coating fluid form, use above-mentioned first transparent coating to form hard coat film and form with coating fluid.
Use the glass lens of the optical material that specific refractory power is high, on surface, formed hard coat film, further on this hard coat film, in case be reflected into object, formed overbrushing layer.In this many coating formations operation, on glass lens base material, produce sometimes distortion, because the impact falling etc. is easily split eyeglass, so between glass lens and hard coat film, be provided with the soft bottom coating of impact-absorbing.
The specific refractory power of bottom coating, if with the specific refractory power of base material not etc., there is sometimes interference fringe, but transparent coating of the present invention forms with in coating fluid, as matrix composition, it is that resin, melamine series resin, ammonia ester are that resin, vibrin, phosphocreatine are the second transparent coating formation coating fluid of the resin of resin etc. that use comprises aforesaid propylene acid, can form the bottom coating with the specific refractory power same degree of base material.
Moreover, form in the situation of such bottom coating, adopt method as described above, after coating coating fluid, solidify tunicle.
Transparent coating of the present invention forms with in coating fluid, for promoting reaction, can contain solidifying agent, in addition, for consistent with the specific refractory power of base material, can contain finely particulate metal oxide, the wettability during further for raising coating, the object that improves the smoothness of the tunicle after solidifying, can contain various tensio-active agents.In addition, only otherwise affect the physical property of cured film, also can add UV light absorber, oxidation inhibitor etc.
In addition, by transparent coating of the present invention, forming the antireflection film of vapor-deposited film that arrange, that comprise inorganic oxide on the tunicle obtaining with coating fluid, be not particularly limited, can use in the past the individual layer of the known vapor-deposited film that comprises inorganic oxide, the antireflection film of multilayer.As the example of this antireflection film, can enumerate such as Japanese kokai publication hei 2-262104 communique, the disclosed antireflection film of Japanese kokai publication sho 56-116003 communique etc.
Shock absorption film, improves shock-resistance.This shock absorption film is the formations such as resin, polyvinyl alcohol resin with polyacrylic resin, Vinyl Acetate Copolymer.
In addition, by transparent coating of the present invention, form the tunicle obtaining with coating fluid, as high refractive index film, can be used in reflectance coating, further, by adding antifog, photochromic, antifouling etc. functional component, also can be used as multifunctional membrane and use.
The optics with the tunicle that comprises application composition of the present invention, outside glasses lens, can also be for the window glass of camera lens, automobile for camera, be attached to the optical filter of liquid-crystal display and plasma display etc. etc.
Embodiment
Embodiment by following, illustrates the present invention, but the present invention is not limited to these embodiment.(Production Example)
Production Example 1
According to the embodiment 2 of Japanese kokai publication hei 10-245224 communique, modulated the water-dispersion colloidal sol of the nuclear particle (A1) that contains titanium dioxide.
(a) operation: by titanium tetrachloride (Sumitomo シ チ ッ Network ス (strain) system: TiO 2conversion concentration 27.2 quality %, Cl32.0 quality %) 293.8g(TiO 2conversion 79.8g) and water 371.6g, be taken to the detachable flask of glass system with book jacket (jacket) of 3 liters, modulated titanium chloride aqueous solution 665g(TiO 2conversion concentration 12.0 quality %).On one side by glass stirring rod processed, stir this aqueous solution and be heated on one side after 50 ℃, on one side cooling one side added aquae hydrogenii dioxidi 950.8g and metallic tin powder (mountain stone metal (strain) is made: trade(brand)name AT-Sn, the No.200) 566.4g of 35 quality %.The interpolation of aquae hydrogenii dioxidi and metallic tin, first slowly adds metallic tin 31.5g(0.265 mole), then slowly add aquae hydrogenii dioxidi 53.8g(0.554 mole).Wait for that this reaction finishes, and slowly adds metallic tin 31.5g(0.265 mole), then slowly add aquae hydrogenii dioxidi 53.8g(0.554 mole).So, by the interpolation of the aquae hydrogenii dioxidi after adding metallic tin, at interval of 5～10 minutes, add up to 17 times repeatedly, after carry out thus (metallic tin 31.5g and aquae hydrogenii dioxidi 53.8g) * 17 times separately add, finally add metallic tin 30.9g, then add aquae hydrogenii dioxidi 36.2g, add up to the separately interpolation of having carried out 18 times.Because reaction is exothermic reaction, by adding metallic tin, the aqueous solution becomes 70～75 ℃, and reaction finishes coolingly to drop to 50～60 ℃ afterwards.Reaction is carried out at 50～75 ℃.The adding proportion of the once amount of hydrogen peroxide and metallic tin is with H 2o 2/ Sn molar ratio computing is 2.09.The time that the interpolation of aquae hydrogenii dioxidi and metallic tin needs is 3.0 hours.After reaction finishes, obtain alkaline titanium chloride-Xi composite salt aqueous solution 3195.6g.Concentration now, as TiO 2+ SnO 2the total concentration converting is 25 quality %.
(b) operation: in the alkaline titanium chloride-Xi composite salt aqueous solution 2870g obtaining in (a) operation, add the ammoniacal liquor of the 28 quality % of 11269g water, 211g, by TiO 2+ SnO 2conversion concentration dilution is to 5 quality %.This aqueous solution is carried out to hydrolysis in 10 hours at 95 ℃, obtain the agglomeration slurries of titanium dioxide-tindioxide composite gel.
(c) operation: by the agglomeration slurries of the titanium dioxide-tindioxide composite gel obtaining in (b) operation, utilize ultrafiltration unit, use the water of approximately 15 liters, repeatedly concentrate the operation with water filling, washing is removed after superfluous ionogen, make its dispergation, obtain acid titanium dioxide-tindioxide Compound Water and disperse colloidal sol 14350g.The primary particle size that the employing transmission electron microscope of titanium dioxide-tindioxide composite gel particle is observed is 4～8nm.
(d) operation: in the acid titanium dioxide-tindioxide complex sol 14350g obtaining in (c) operation, add 137g Isopropylamine, be modulated to after alkalescence, utilize ultrafiltration unit, use the water of approximately 24 liters, repeatedly concentrate and the operation of water filling, superfluous ionogen is removed in washing, obtains alkaline titanium dioxide-tindioxide Compound Water and disperses colloidal sol 14600g.Further to 200 milliliters of anionite-exchange resin (オ Le ガ ノ (strain) system: logical liquid in packed column (column) ア ン バ ー ラ イ ト (registered trademark) IRA-410), obtains alkaline titanium dioxide-tindioxide water-dispersion colloidal sol 15500g that negatively charged ion has roughly been removed is housed.With Rotary Evaporators, this colloidal sol is under reduced pressure concentrated to the water-dispersion colloidal sol 7kg of the nuclear particle (A1) that obtains containing titanium dioxide.(TiO now 2+ SnO 2) conversion concentration is 10 quality %.The primary particle size of being observed by transmission electron microscope of the nuclear particle that contains titanium dioxide (A1) is 4～8nm.By the colloidal sol obtaining, carry out the X-ray diffraction analysis that makes its powder being dried at 110 ℃, confirm as rutile-type crystallization.
Production Example 2
According to the embodiment 2 of Japanese kokai publication hei 10-310429 communique, modulated the water-dispersion colloidal sol of the nuclear particle (A2) that contains titanium dioxide.
(a) operation: by titanium tetrachloride (TiO 227.2 quality %, Cl32.0 quality %, Sumitomo シ チ ッ Network ス (strain) system convert) 587.5g(TiO 2conversion 159.8g), carbonic acid zirconium white (ZrO 2the 43.0 quality % that convert, first rare element chemistry (strain) system) 114.6g(ZrO 2conversion 49.2g) and water 629.6g, be taken to the detachable flask of glass system with book jacket of 3 liters, modulated the mixed aqueous solution 1331.7g(TiO of titanium chloride and basic zirconium chloride 212.0 quality %, ZrO convert 23.7 quality % convert).On one side by glass stirring rod processed, stir this aqueous solution and be heated on one side after 60 ℃, on one side cooling one side added aquae hydrogenii dioxidi 358.0g and metallic tin powder (mountain stone metal (strain) is made: trade(brand)name AT-Sn, the No.200) 190.0g of 35 quality %.The interpolation of aquae hydrogenii dioxidi and metallic tin, slowly adds aquae hydrogenii dioxidi 35.8g(0.37 mole at first), then slowly add metallic tin 19.0g(0.16 mole).After this reaction finishes about 5～10 minutes, slowly add hydrogen peroxide 35.8g(0.37 mole), then slowly add metallic tin 19.0g(0.16 mole).So, by being connected on the interpolation of the metallic tin after hydrogen peroxide, at interval of 5～10 minutes, add up to 10 times repeatedly, carried out thus (hydrogen peroxide 35.8g and metallic tin 19.0g) * 10 times separately add.Because reaction is exothermic reaction, by adding metallic tin, become 80～85 ℃, reaction finishes coolingly to drop to 60～70 ℃ afterwards.Temperature of reaction is carried out at 60～85 ℃.The adding proportion of hydrogen peroxide and metallic tin is with H 2o 2/ Sn molar ratio computing is 2.31.The time that the interpolation of aquae hydrogenii dioxidi and metallic tin needs is 2.5 hours.Moreover by reaction, water evaporation, has therefore carried out supplementing of appropriate water.After reaction finishes, obtain faint yellow transparent alkaline titanium chloride-zirconium-Xi composite salt aqueous solution 1780g.In the alkaline titanium chloride-zirconium-Xi composite salt aqueous solution obtaining, titanium composition is as TiO 2conversion concentration is 8.98 quality %, and zirconium composition is as ZrO 2conversion concentration is 2.76 quality %, and tin composition is as SnO 2conversion concentration is 13.55 quality %, ZrO 2/ TiO 2mol ratio is 0.2, TiO 2/ (ZrO 2+ SnO 2) mol ratio is 1.0.In addition, (Ti+Zr+Sn)/Cl mol ratio is 0.76.
(b) operation: in the alkaline titanium chloride-zirconium-Xi composite salt aqueous solution 1780g obtaining in (a) operation, add ammoniacal liquor 259g, the water 6964g of 28 quality %, by TiO 2+ ZrO 2+ SnO 2conversion concentration dilution is to 5 quality %.This aqueous solution is carried out to hydrolysis in 12 hours at 95～98 ℃, obtain the agglomeration slurries of titanium dioxide-zirconium dioxide-tindioxide composite gel particle.
(c) operation: by the agglomeration slurries of the titanium dioxide-zirconium dioxide-tindioxide composite gel particle obtaining in (b) operation, adopt ultrafiltration unit, use the water of approximately 20 liters, repeatedly concentrate the operation with water filling, washing is removed after superfluous ionogen, make its dispergation, obtain the water-dispersion colloidal sol 8400g of acid titanium dioxide-zirconium dioxide-tindioxide composite gel particle.The primary particle size that the employing transmission electron microscope of titanium dioxide-tindioxide composite gel particle is observed is 4～8nm.
(d) operation: in the complex sol 9000g of the acid titanium dioxide-zirconium dioxide-tindioxide colloidal particle obtaining in (c) operation, add Isopropylamine 27.0g, be modulated to after alkalescence, adopt ultrafiltration unit, use the water of approximately 20 liters, repeatedly concentrate and the operation of water filling, superfluous ionogen is removed in washing, obtains the water-dispersion colloidal sol 8000g of alkaline titanium dioxide-zirconium dioxide-tindioxide composite gel particle.This colloidal sol, to logical liquid in the packed column of 500 milliliters of anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed, is obtained to the water-dispersion colloidal sol 9050g of alkaline titanium dioxide-zirconium dioxide-tindioxide composite gel particle that negatively charged ion has roughly been removed.Adopt ultrafiltration unit to concentrate this colloidal sol, obtain the concentrated colloidal sol 3100g of water-dispersion of titanium dioxide-zirconium dioxide-tindioxide composite gel particle.The colloidal sol obtaining, proportion is 1.140, viscosity is that 10.3mPas, pH value are 10.31, specific conductivity is 1105 μ s/cm, TiO 2conversion concentration is 5.18 quality %, ZrO 2conversion concentration is 1.58 quality %, SnO 2the primary particle size that conversion concentration is 7.7 quality %, obtained by transmission electron microscope is 4～8nm.Titanium dioxide-the zirconium dioxide obtaining-tindioxide composite gel particle is made to the nuclear particle (A2) that contains titanium dioxide.By the colloidal sol obtaining, carry out the X-ray diffraction analysis that makes its powder being dried at 110 ℃, confirm as the mixture of rutile-type crystallization and anatase octahedrite crystallization.
Production Example 3
In the container of 3 liters, pour pure water 1169g into, under agitation add the emerging product of oxalic acid dihydrate 151g(space portion (strain) system), phthalandione four isopropyl ester 227g(are with TiO 2conversion contains 64g, Northeast chemistry (strain) system), 25 quality % tetramethylammonium hydroxide aqueous solution 582g(chemical industry (strain) system of rubbing more).The mixing solutions obtaining, the mol ratio of oxalic acid/titanium atom is 1.5, the mol ratio of Tetramethylammonium hydroxide/oxalic acid is 1.33.By this mixing solutions 2131g under atmospheric pressure, in open system, with 88～92 ℃, keep 3 hours, the Virahol producing as byproduct is removed in distillation, has modulated the aqueous solution 1937g that contains titanium.To the aqueous solution that contains titanium obtaining, add pure water 194g, the TiO of the aqueous solution that modulation contains titanium 2conversion concentration is 3.0 quality %.The pH value of the aqueous solution that contains titanium after concentration adjustment is 4.7, and specific conductivity is 31.4mS/cm.In the stainless steel autoclave of 3L (autoclave) container, pour the above-mentioned aqueous solution 2131g that contains titanium into, at 140 ℃, carry out 5 hours hydrothermal treatment consists.Be cooled to after room temperature, the solution after the hydrothermal treatment consists of taking-up is the water-dispersion colloidal sol of the colloidal tio 2 particle that the transparency is high.The colloidal sol obtaining, proportion is 1.037, pH value is 3.8, specific conductivity is 35.7mS/cm, TiO 2concentration be 3.0 quality %, Tetramethylammonium hydroxide concentration be 6.8 quality %, concentration of oxalic acid be 5.1 quality %, dynamic light scattering method particle diameter (utilizing the コ ー ルタ ー N5 of company to measure) for 12nm, viscosity be 3.2mPas(B type viscometer), during transmission electron microscope observes, observe the roughly spherical particle of primary particle size 5～8nm.The colloidal sol obtaining is carried out to the X-ray diffraction analysis that makes its powder being dried at 110 ℃, confirm as Detitanium-ore-type crystallization.The colloidal tio 2 particle obtaining is made to the nuclear particle (A3) that contains titanium dioxide.
Production Example 4
As described below, modulate the nuclear particle (A4) that contains titanium dioxide and disperseed colloidal sol.In the container of 2 liters, add pure water 197g, under agitation added tin oxalate solution 269g(with SnO 2conversion contains 75g, with oxalic acid, converts and to contain 67g), phthalandione four isopropyl ester 142g(are with TiO 2conversion contains 40g), oxalic acid dihydrate 73g(is with the oxalic acid 52g that converts), 25 quality % tetramethylammonium hydroxide aqueous solution 319g.The mixing solutions obtaining, the mol ratio of oxalic acid/titanium atom is 1.3, the mol ratio of Tetramethylammonium hydroxide/titanium atom is 1.75.By this mixing solutions 1000g, at 80 ℃, keep 2 hours, further decompression keeps 2 hours to 580 holders (Torr), has modulated titanium mixing solutions.The pH value of the titanium mixing solutions after modulation is 5.1, specific conductivity is 30.9mS/cm, TiO 2concentration is 4.0 quality %.In the glass lined autoclave vessel of 3 liters, add above-mentioned titanium mixing solutions 1000g, at 140 ℃, carry out 5 hours hydrothermal treatment consists.After cool to room temperature, the solution after the hydrothermal treatment consists of taking-up is the water-dispersion colloidal sol of the colloidal tio 2 particle of light oyster white.The colloidal sol obtaining, pH value is 3.9, specific conductivity is 32.6mS/cm, TiO 2concentration is that 4.0 quality %, Tetramethylammonium hydroxide concentration are that 8.0 quality %, oxalic acid are that 5.9 quality %, dynamic light scattering method particle diameter are during 16nm, transmission electron microscope are observed, and observes the oval particle of primary particle size 5～15nm.The colloidal sol obtaining is carried out to the X-ray diffraction analysis that makes its powder being dried at 110 ℃, confirm as rutile-type crystallization.The colloidal tio 2 particle obtaining is made to the nuclear particle (A4) that contains titanium dioxide.
Production Example 5
Using potassium silicate aqueous solution (as SiO 2contain 19.9 quality %, daily output chemical industry (strain) system) 35.6kg, after diluting, adds 48 quality % potassium hydroxide aqueous solution 18.1kg and antimonous oxide (as Sb with pure water 330.0kg 2o 3contain 99 quality %, three Guo Jing And-chain (strain) systems) 3.2kg, under agitation add the 35 quality % aquae hydrogenii dioxidis of 2.2kg, at 93 ℃, make its reaction 1 hour, obtain thus the silicic acid potassium antimonate aqueous solution.By the silicic acid potassium antimonate aqueous solution 427.5g obtaining is diluted with pure water 1kg, to the logical liquid of the packed column that is filled with hydrogen type cation exchange resin (ア ン バ ー ラ イ ト (registered trademark) IR-120B), obtain silicon-dioxide-antimony peroxide composite oxides colloidal particle water-dispersion colloidal sol (pH value is 2.1, as Sb 2o 5contain 0.64 quality %, as SiO 2contain 1.26 quality %, SiO 2/ Sb 2o 5mass ratio is 2.0) 2703g.Then, to the water-dispersion colloidal sol obtaining, add Diisopropylamine 10.2g.The colloidal sol obtaining is the water-dispersion colloidal sol of alkaline silicon-dioxide-antimony peroxide composite oxides colloidal particle, and pH value is 8.2.The water-dispersion colloidal sol obtaining, observes the colloidal particle below primary particle size 5nm.
Production Example 6
Using JIS3 water glass (as SiO 2containing 29.8 quality %, Fuji chemistry (strain) system) 77.2g is dissolved in pure water 1282g, then dissolved sodium stannate NaSnO 3h 2o(is as SnO 2contain 55.1 quality %, clear and chemical industry (strain) system) 20.9g.By the aqueous solution obtaining is passed through in the packed column of having filled hydrogen type cation exchange resin (ア ン バ ー ラ イ ト (registered trademark) IR-120B), obtain acid silicon-dioxide-tindioxide composite gel particle (B1) water-dispersion colloidal sol (pH value is 2.4, as SnO 2contain 0.44 quality %, as SiO 2contain 0.87 quality %, SiO 2/ SnO 2mass ratio 2.0) 2634g.Then in the water-dispersion colloidal sol obtaining, add Diisopropylamine 6.9g.The colloidal sol obtaining is the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1), and pH value is 8.0.This water-dispersion colloidal sol, adopts transmission electron microscope to observe the colloidal particle of the primary particle size below 5nm.
Embodiment 1
Using basic zirconium chloride (as ZrO 2contain 21.19 quality %, first rare element chemistry industry (strain) system) pure water 429.2g dilution for 70.8g, modulation zirconium oxychloride aqueous solution 500g(is as ZrO 2contain 3.0 quality %), under agitation add in Production Example 1 the water-dispersion colloidal sol 1000g of the nuclear particle that contains titanium dioxide (A1) of modulation.Then be heated to 95 ℃, be hydrolyzed, obtain having formed on surface the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A1) of the thin film layer of zirconium dioxide.The water-dispersion colloidal sol obtaining, pH value is 1.2, total metal oxide concentration is 20 quality %, during transmission electron microscope is observed, observes the colloidal particle of primary particle size 4～8nm.The water-dispersion colloidal sol 1455g obtaining is under agitation added in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulating in the Production Example 6 of 2634g.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 95 ℃, the water-dispersion colloidal sol after logical liquid was heated after 3 hours, concentrated by ultra-filtration embrane method, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The total metal oxide concentration of the water-dispersion colloidal sol obtaining is 20 quality %, and the primary particle size of observing by transmission electron microscope of this colloidal sol is 4～10nm.Then, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1) containing.This methyl alcohol disperses colloidal sol, and total metal oxide concentration is that 30 quality %, viscosity are 3.2mPas, the particle diameter (DLS particle diameter: adopt N4PLUS processed of BECKMANCOULTER company to measure) that obtained by dynamic light scattering method is that 32nm, moisture are 1.2 quality %.
Embodiment 2
Using basic zirconium chloride (as ZrO 2contain 21.19 quality %, first rare element chemistry industry (strain) system) pure water 429.2g dilution for 70.8g, modulation zirconium oxychloride aqueous solution 500g(is as ZrO 2contain 3.0 quality %), under agitation add in Production Example 2 the water-dispersion colloidal sol 1298.7g of the nuclear particle that contains titanium dioxide (A2) of modulation.Then by being heated to 95 ℃, be hydrolyzed, obtain having formed on surface the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A2) of the thin film layer of zirconium dioxide.The water-dispersion colloidal sol obtaining, pH value is 1.2, total metal oxide concentration is 20 quality %, during the transmission electron microscope of this colloidal sol is observed, observes the colloidal particle of primary particle size 4～8nm.The water-dispersion colloidal sol 1764g obtaining is under agitation added in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulating in the Production Example 6 of 2634g.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 95 ℃, the water-dispersion colloidal sol after logical liquid was heated after 3 hours, concentrated by ultra-filtration embrane method, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The total metal oxide concentration of the water-dispersion colloidal sol obtaining is 20 quality %, this colloidal sol by the observable primary particle size of transmission electron microscope, be 4～10nm.Then, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-tindioxide composite gel particle (B1) containing.This methyl alcohol disperses colloidal sol, and total metal oxide concentration is that 30 quality %, viscosity are that 3.2mPas, DLS particle diameter are that 36nm, moisture are 1.5 quality %.Embodiment 3
Using basic zirconium chloride (as ZrO 2contain 21.19 quality %, first rare element chemistry industry (strain) system) pure water 217g dilution for 35.8g, modulation zirconium oxychloride aqueous solution 253g(is as ZrO 2contain 3.0 quality %), under agitation add in Production Example 3 the water-dispersion colloidal sol 1331g of the nuclear particle that contains titanium dioxide (A3) of modulation.Then by being heated to 95 ℃, be hydrolyzed, obtain having formed on surface the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A3) of the thin film layer of zirconium dioxide.The water-dispersion colloidal sol obtaining, pH value is 1.2, total metal oxide concentration is 20 quality %, during the transmission electron microscope of this colloidal sol is observed, observes the colloidal particle of primary particle size 4～8nm.The water-dispersion colloidal sol obtaining is under agitation added in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulating in the Production Example 6 of 1090g.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 150 ℃, the water-dispersion colloidal sol after logical liquid was heated after 3 hours, concentrated by ultra-filtration embrane method, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A3) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The total metal oxide concentration of the water-dispersion colloidal sol obtaining is 20 quality %, this colloidal sol by the observable primary particle size of transmission electron microscope, be 5～10nm.Then, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A3) and silicon-dioxide-tindioxide composite gel particle (B1) containing.This methyl alcohol disperses colloidal sol, and total metal oxide concentration is that 30 quality %, viscosity are that 2.2mPas, DLS particle diameter are that 22nm, moisture are 1.0 quality %.
Embodiment 4
Using basic zirconium chloride (as ZrO 2contain 21.19 quality %, first rare element chemistry industry (strain) system) pure water 217g dilution for 35.9g, modulation zirconium oxychloride aqueous solution 253g(is as ZrO 2contain 3.0 quality %), under agitation add in Production Example 4 the water-dispersion colloidal sol 1000g of the nuclear particle that contains titanium dioxide (A4) of modulation.Then by being heated to 95 ℃, be hydrolyzed, obtain having formed on surface the water-dispersion colloidal sol of the nuclear particle that contains titanium dioxide (A4) of the thin film layer of zirconium dioxide.The water-dispersion colloidal sol obtaining, pH value is 1.2, total metal oxide concentration is 20 quality %, during the transmission electron microscope of this colloidal sol is observed, observes the colloidal particle of primary particle size 5～15nm.The water-dispersion colloidal sol 1231g obtaining is under agitation added in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulating in the Production Example 6 of 1090g.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 150 ℃, the water-dispersion colloidal sol heating after logical liquid, after 3 hours, is obtained to the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The water-dispersion colloidal sol obtaining is 2877g, and total metal oxide concentration is 2.1 quality %, this colloidal sol by the observable primary particle size of transmission electron microscope, be 5～18nm.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The methyl alcohol obtaining disperses colloidal sol, and total metal oxide concentration is that 30 quality %, viscosity are that 2.0mPas, DLS particle diameter are that 24nm, moisture are 0.9 quality %.
Embodiment 5
Replace zirconium oxychloride aqueous solution 500g, used the water-dispersion colloidal sol 1211g of silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 1 in addition, obtain between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1), being formed with the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that comprises silicon-dioxide-antimony peroxide composite oxides intermediate thin rete containing.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 3.1mPas, DLS particle diameter are that 32nm, moisture are 1.1 quality %.
Embodiment 6
Replace zirconium oxychloride aqueous solution 500g, used the water-dispersion colloidal sol 1211g of silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 2 in addition, obtain between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-tindioxide composite gel particle (B1), being formed with the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that comprises silicon-dioxide-antimony peroxide composite oxides intermediate thin rete containing.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 3.3mPas, DLS are that particle diameter 35nm, moisture are 2.0 quality %.
Embodiment 7
Replace zirconium oxychloride aqueous solution 253g, used the water-dispersion colloidal sol 653g of silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 3 in addition, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A3) and silicon-dioxide-tindioxide composite gel particle (B1) containing.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A3) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 1.6mPas, DLS particle diameter are that 18nm, moisture are 1.1 quality %.
Embodiment 8
Replace zirconium oxychloride aqueous solution 253g, used the water-dispersion colloidal sol 653g of silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 3 in addition, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-tindioxide composite gel particle (B1) containing.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide composite oxides between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-tindioxide composite gel particle (B1) containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 2.4mPas, DLS particle diameter are that 21nm, moisture are 1.3 quality %.
Comparative example 1
By the water-dispersion colloidal sol 1150g of the nuclear particle that contains titanium dioxide (A1) of modulation in Production Example 1, under agitation add in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulating in the Production Example 6 of 2634g.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 95 ℃, the water-dispersion colloidal sol after logical liquid was heated after 3 hours, concentrated by ultra-filtration embrane method, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle being formed by titanium dioxide nuclear particle (A1) and the coating that comprises silicon-dioxide-tindioxide composite gel particle (B1).The total metal oxide concentration of the water-dispersion colloidal sol obtaining is 16.5 quality %, this colloidal sol by the observable primary particle size of transmission electron microscope, be 4～10nm.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, and the methyl alcohol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that obtains being formed by titanium dioxide nuclear particle (A1) and the coating that comprises silicon-dioxide-tindioxide composite gel particle (B1) disperses colloidal sol.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 3.8mPas, DLS particle diameter are that 41nm, moisture are 0.9 quality %.
Comparative example 2
The water-dispersion colloidal sol 1090g that replaces alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulation in Production Example 6, used the water-dispersion colloidal sol 747g of alkaline silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 2 in addition, obtain containing the water-dispersion colloidal sol that contains silicon-dioxide-antimony peroxide composite oxides coating titanium dioxide metal oxide particle that between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-antimony peroxide composite oxides colloidal particle, formation comprises zirconic intermediate thin rete.This colloidal sol by the observable primary particle size of transmission electron microscope, be 4～10nm.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-antimony peroxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-antimony peroxide composite gel particle containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 3.4mPas, DLS particle diameter are that 44nm, moisture are 0.7 quality %.
Comparative example 3
Water-dispersion colloidal sol 1666g by the nuclear particle that contains titanium dioxide (A3) of modulation in Production Example 3, under agitation adds in the water-dispersion colloidal sol of alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulation in 1317g Production Example 6.Then, to the logical liquid of packed column that 500 milliliters, anionite-exchange resin (ア ン バ ー ラ イ ト (registered trademark) IRA-410, オ Le ガ ノ (strain) system) is housed.Then, at 95 ℃, the water-dispersion colloidal sol after logical liquid was heated after 3 hours, concentrated by ultra-filtration embrane method, obtain the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle being formed by titanium dioxide nuclear particle (A3) and the coating that comprises silicon-dioxide-tindioxide composite gel particle (B1).The total metal oxide concentration of the water-dispersion colloidal sol obtaining is 16.8 quality %, this colloidal sol by the observable primary particle size of transmission electron microscope, be 5～10nm.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, and the methyl alcohol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that obtains being formed by titanium dioxide nuclear particle (A3) and the coating that comprises silicon-dioxide-tindioxide composite gel particle (B1) disperses colloidal sol.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 1.6mPas, DLS particle diameter are that 13nm, moisture are 2.5 quality %.
Comparative example 4
The water-dispersion colloidal sol 1090g that replaces alkaline silicon-dioxide-tindioxide composite gel particle (B1) of modulation in Production Example 6, used the water-dispersion colloidal sol 747g of alkaline silicon-dioxide-antimony peroxide composite oxides colloidal particle of modulation in Production Example 5, carry out similarly to Example 4 in addition, obtain containing the water-dispersion colloidal sol that contains silicon-dioxide-antimony peroxide composite oxides coating titanium dioxide metal oxide particle that between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-antimony peroxide composite oxides colloidal particle, formation comprises zirconic intermediate thin rete.This colloidal sol by the observable primary particle size of transmission electron microscope, be 5～18nm.Further, the dispersion medium of the water-dispersion colloidal sol obtaining is replaced as to methyl alcohol with Rotary Evaporators, obtains the methyl alcohol that the contains silicon-dioxide-antimony peroxide composite oxides coating titanium dioxide metal oxide particle dispersion colloidal sol that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-antimony peroxide composite gel particle containing.The methyl alcohol obtaining disperses colloidal sol, and concentration is that 30 quality %, viscosity are that 2.1mPas, DLS particle diameter are that 18nm, moisture are 1.7 quality %.
Embodiment 9
To possessing in the container of glass system of magnetic stirring apparatus, add γ-glycidyl ether oxygen base propyl trimethoxy silicane 55.8 mass parts, while stir, use 3 hours and drip 0.01 centinormal 1 hydrochloric acid 19.5 mass parts.After dropping finishes, carry out the stirring of 0.5 hour, obtain the partial hydrolystate of γ-glycidyl ether oxygen base propyl trimethoxy silicane.Then, the methyl alcohol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide in embodiment 1 between the nuclear particle that is containing titanium dioxide (A1) obtaining and silicon-dioxide-tindioxide composite gel particle (B1) is disperseed to colloidal sol (convert and contain 30 quality % with total metal oxide) 151.0 mass parts, ethylene glycol butyl ether 65 mass parts, be further used as aluminium acetylacetonate 0.9 mass parts of solidifying agent, add in partial hydrolystate 75.3 mass parts of above-mentioned γ-glycidyl ether oxygen base propyl trimethoxy silicane, after fully stirring, filter, make transparent coating formation coating fluid.In addition, by the industrial pharmacy of commercially available water dispersible polyurethane latex (ス ー パ ー Off レ ッ Network ス (registered trademark) 170: the first (strain) system, solid component concentration 30 quality %) 151.0 mass parts, pure water 74 mass parts mix, and have modulated stratum basale coating liquid.
(formation of cured film)
Prepare commercially available refractive index n d=1.59 polycarbonate plate, is first coated with above-mentioned stratum basale surface-coated composition with method of spin coating thereon, with 100 ℃ of heat treated, within 30 minutes, makes its formation film.Further, coating transparent coating formation coating fluid, with 120 ℃ of heat treated 2 hours, makes curing of coating.Evaluation result is shown in table 1.
Embodiment 10
Except having used the methyl alcohol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide in embodiment 2 between the nuclear particle that is containing titanium dioxide (A2) that obtains and silicon-dioxide-tindioxide composite gel particle (B1) to disperse colloidal sol (convert and contain 30 quality % with total metal oxide) 151.5 mass parts, to carry out similarly to Example 10.Evaluation result is shown in table 1.
Embodiment 11
Except having used the methyl alcohol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide in embodiment 3 between the nuclear particle that is containing titanium dioxide (A3) that obtains and silicon-dioxide-tindioxide composite gel particle (B1) to disperse colloidal sol (convert and contain 30 quality % with total metal oxide) 151 mass parts, to carry out similarly to Example 10.Evaluation result is shown in table 1.
Embodiment 12
What obtain obtaining in embodiment 4 is containing the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises zirconium dioxide between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-tindioxide composite gel particle (B1).Except having used water-dispersion colloidal sol (convert and contain 30 quality % with total metal oxide) 151 mass parts that obtain, carry out similarly to Example 10.Evaluation result is shown in table 1.
Embodiment 13
In having used embodiment 5, obtained containing the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle (be scaled total metal oxide and contain 30 quality %) 151 mass parts that are formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide between the nuclear particle of titanium dioxide (A1) and silicon-dioxide-tindioxide composite gel particle (B1), carry out similarly to Example 10.Evaluation result is shown in table 1.
Embodiment 14
In having used embodiment 6, obtained containing the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle (be scaled total metal oxide and contain 30 quality %) 151 mass parts that are formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide between the nuclear particle of titanium dioxide (A2) and silicon-dioxide-tindioxide composite gel particle (B1), carry out similarly to Example 10.
Embodiment 15
In having used embodiment 7, obtained containing the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide between the nuclear particle of titanium dioxide (A3) and silicon-dioxide-tindioxide composite gel particle (B1) (convert and contain 30 quality % with total metal oxide) 151 mass parts, carry out similarly to Example 10.Evaluation result is shown in table 1.
Embodiment 16
In having used embodiment 8, obtained containing the water-dispersion colloidal sol that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide metal oxide particle that is formed with the intermediate thin rete that comprises silicon-dioxide-antimony peroxide between the nuclear particle of titanium dioxide (A4) and silicon-dioxide-tindioxide composite gel particle (B1) (convert and contain 30 quality % with total metal oxide) 151 mass parts, carry out similarly to Example 10.Evaluation result is shown in table 1.
Comparative example 5
The colloidal sol using in alternate embodiment 10, is used the colloidal sol of making in comparative example 1, similarly carries out.Evaluation result is shown in table 1.
Comparative example 6
The colloidal sol using in alternate embodiment 10, is used the colloidal sol of making in comparative example 2, similarly carries out.Evaluation result is shown in table 1.
Comparative example 7
The colloidal sol using in alternate embodiment 10, is used the colloidal sol of making in comparative example 3, similarly carries out.Evaluation result is shown in table 1.
Comparative example 8
The colloidal sol using in alternate embodiment 10, is used the colloidal sol of making in comparative example 4, similarly carries out.Evaluation result is shown in table 1.
Moreover, there is the optics of the cured film obtaining in embodiment and comparative example, adopt measuring method as follows to measure all physical property.
(1) atmospheric exposure test
For the optics obtaining, at high pressure mercury vapour lamp (ア ー Network, make UV-800 processed of institute's (strain)) under carry out the exposure of 100 hours, the appearance change with the optics after visual judgement exposure, judges.
A: nondiscoloration completely.
B: variable color hardly.
C: variable color is strong.
(2) resistance to cracking test
The test film outward appearance of having used in the light fastness test of visual observation (1), judges.
A: do not ftracture completely.
B: almost do not ftracture.
C: a little cracking occurs.
D: comprehensively ftracture.
(3) scuff resistance test
With Steel Wool #0000 wiping cured film surface, there is abrasive difficulty in visual judgement.Judgment standard is as follows.
A: at all cannot confirm to have wound
B: can confirm some scars
C: can confirm many obvious scars
(4) transparency test
In darkroom, under luminescent lamp, visual investigation cured film has or not dirt.Judgment standard is as follows.
A: almost do not occur dirty
B: dirty degree is no problem degree as transparent cured film
C: obviously show albefaction
(5) long-term stable experiment
Each transparent coating of modulation in embodiment 9～16, comparative example 5～8 is formed with coating fluid and preserved after 60 days at 10 ℃, similarly form transparent coating with each embodiment 9～16, comparative example 5～8, carry out the evaluation of the atmospheric exposure test of (1).With A, B, the evaluation of C three phases, just modulated the difference that transparent coating forms with the transparent coating that formed after coating fluid and is used in the transparent coating that 10 ℃ of coating fluids of preserving after 60 days have formed.
A: cannot confirm difference.
B: can confirm has the low of a little performance.
C: can confirm has the low of significant performance.
Figure BDA0000462906270000361
Embodiments of the invention 1～8, scuff resistance, adaptation, the transparency and have excellent weather resistance.Comparative example 1～4, can not say enough aspect scuff resistance, the transparency and weathering resistance.

Claims (12)

1. a metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide, it has the nuclear particle (A) that contains titanium dioxide and by the coating of this nuclear particle (A) coating, the mass ratio that described coating comprises silicon-dioxide/tindioxide is silicon-dioxide-tindioxide composite oxides colloidal particles (B) of 0.1～5.0, and 1 layer of above intermediate thin rete forms between the described nuclear particle that contains titanium dioxide (A) and the described coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B), described intermediate thin rete comprises and is selected from Si, Al, Sn, Zr, Zn, Sb, Nb, the oxide compound of at least a kind of element in Ta and W, composite oxides, or any a kind of the mixture of this oxide compound and these composite oxides.
2. the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide according to claim 1, described in contain titanium dioxide nuclear particle (A) in content of titanium dioxide with TiO 2be scaled 5～100 quality %, the amount of the described coating that comprises silicon-dioxide-tindioxide composite oxides colloidal particles (B) is with respect to the quality of the described nuclear particle that contains titanium dioxide (A), the scope 0.01～1.0.
3. the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide according to claim 1 and 2, the described nuclear particle that contains titanium dioxide (A), for comprising the nuclear particle that is selected from least a kind of element in Si, Al, Sn, Zr, Zn, Sb, Nb, Ta and W.
4. according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of claim 1～3, described in contain titanium dioxide the crystal formation of nuclear particle (A) be rutile-type.
5. according to the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of claim 1～4, in surface bonding, there are silicoorganic compound or amine compound.
6. a metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide disperses colloidal sol, that the metal oxide particle that metal oxide particle is scattered in dispersion medium disperses colloidal sol, described metal oxide particle is the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one of claim 1～5, and described dispersion medium is the mixed solvent of water, organic solvent or water and organic solvent.
7. a transparent coating formation coating fluid, comprise metal oxide particle and matrix forming component, the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one that described metal oxide particle contains claim 1～5, described matrix forming component contains at least a kind that is selected from silicoorganic compound, the hydrolyzate of these silicoorganic compound and the partial condensate of this hydrolyzate representing with following formula I
R 1 aR 2 bSi（OR 3） 4-（a+b） （Ⅰ）
In formula, R 1represent alkyl, vinyl, the methacryloxy of carbonatoms 1～10 or there is the organic group of sulfydryl, amino or epoxy group(ing), R 2the alkyl that represents carbonatoms 1～4, R 3the alkyl or the acyl group that represent carbonatoms 1～8, a, b represent 0 or 1.
8. a transparent coating formation coating fluid, comprise metal oxide particle and matrix forming component, the metal oxide particle that contains silicon-dioxide-tindioxide composite oxides coating titanium dioxide described in any one that described metal oxide particle contains claim 1～5, described matrix forming component contains at least a kind of resin being selected from heat-curing resin, thermoplastic resin and uv curing resin.
9. described transparent coating formation coating fluid according to Claim 8, described matrix forming component is that polyester based resin or ammonia ester are resin.
10. a base material that adheres to transparent coating, has right to use and requires the transparent coating described in 7～9 any one to form the transparent coating forming with coating fluid on surface.
11. 1 kinds of base materials that adhere to transparent coating, on surface, there is right to use and require the transparent coating described in 8 or 9 to form the bottom coating forming with coating fluid, and further there is the hard coat film that right to use requires the transparent coating formation described in 7 to form with coating fluid thereon.
12. according to the base material that adheres to transparent coating described in claim 10 or 11, on described transparent coating or hard coat film, further has antireflection film.
CN201280037509.2A 2011-06-03 2012-06-01 The metal oxide particle of titanium dioxide is coated to containing silicon-dioxide-tindioxide composite oxides Active CN103717535B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2011-125259 2011-06-03
JP2011125259 2011-06-03
PCT/JP2012/064296 WO2012165620A1 (en) 2011-06-03 2012-06-01 Metal oxide particles containing titanium oxide coated with silicon dioxide-tin(iv) oxide complex oxide

Publications (2)

Publication Number Publication Date
CN103717535A true CN103717535A (en) 2014-04-09
CN103717535B CN103717535B (en) 2016-02-10

Family

ID=47259471

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201280037509.2A Active CN103717535B (en) 2011-06-03 2012-06-01 The metal oxide particle of titanium dioxide is coated to containing silicon-dioxide-tindioxide composite oxides

Country Status (8)

Country Link
US (2) US20140199554A1 (en)
EP (1) EP2724984B1 (en)
JP (1) JP5896178B2 (en)
KR (1) KR101907882B1 (en)
CN (1) CN103717535B (en)
HU (1) HUE031805T2 (en)
TW (1) TWI534088B (en)
WO (1) WO2012165620A1 (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104151868A (en) * 2014-07-10 2014-11-19 池州市英派科技有限公司 Modified nano-titanium dioxide with reinforced photocatalytic effect and preparation method thereof
CN105785590A (en) * 2016-05-20 2016-07-20 四川梅塞尔科技有限公司 Preparation method and products for color-changing wearable self-cleaning concave lens
CN107272333A (en) * 2016-03-31 2017-10-20 日挥触媒化成株式会社 Surface-treated metal oxide sol
CN108033486A (en) * 2017-12-15 2018-05-15 河北麦森钛白粉有限公司 A kind of preparation method of conductive mesoporous nano titanium dioxide
CN109071258A (en) * 2016-03-31 2018-12-21 日产化学工业株式会社 It is combined with the inorganic oxide particle, its dispersion in organic solvent and envelope formation composition of amphipathic organic silane compound
CN111699157A (en) * 2017-12-11 2020-09-22 日产化学株式会社 Inorganic oxide particles coated with silane compound containing nitrogen ring, and coating composition
CN112739871A (en) * 2018-09-21 2021-04-30 克洛诺斯国际有限公司 Laminate pigments with spacing properties and high UV-ashing stability
CN112752802A (en) * 2018-09-27 2021-05-04 日产化学株式会社 Acrylic coating composition containing inorganic oxide particles
CN113166343A (en) * 2018-11-21 2021-07-23 日产化学株式会社 Reactive silicone composition and cured product thereof
CN114531854A (en) * 2020-07-07 2022-05-24 日产化学株式会社 Inorganic oxide sol dispersed in hydrocarbon and process for producing the same
CN115335329A (en) * 2020-03-26 2022-11-11 帝化株式会社 Rutile titanium oxide organosol, method for producing rutile titanium oxide organosol, and composition for forming high-refractive-index coating film and optical element using rutile titanium oxide organosol
CN116891658A (en) * 2022-04-06 2023-10-17 东洋油墨Sc控股株式会社 Protective film, housing, and electronic device
CN116891658B (en) * 2022-04-06 2024-10-29 爱天思株式会社 Protective film, housing, and electronic device

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102781821B (en) * 2010-01-19 2015-01-07 日产化学工业株式会社 Silane surface-treated metal oxide fine particles and production method for same
JP2014205811A (en) * 2013-04-16 2014-10-30 国立大学法人東北大学 Ultraviolet ray shielding film
CN103627219B (en) * 2013-10-25 2015-04-22 浙江理工大学 Organic modification method of Halloysite nanotubes
JP6354409B2 (en) * 2014-07-14 2018-07-11 住友大阪セメント株式会社 Metal oxide particle dispersion, metal oxide particle-containing composition, coating film, display device
WO2016017603A1 (en) * 2014-07-30 2016-02-04 コニカミノルタ株式会社 Method for producing vanadium dioxide-containing particle and dispersion
KR102628748B1 (en) 2015-04-30 2024-01-24 닛산 가가쿠 가부시키가이샤 Coating composition and optical member
US10676643B2 (en) 2016-03-31 2020-06-09 Nissan Chemical Industries, Ltd. Coating film-forming composition and process for producing the same
CN107162044B (en) * 2017-06-23 2018-09-14 广州特种承压设备检测研究院 A kind of compound nuclear shell structure nano powder preparation method
US11820917B2 (en) 2017-12-11 2023-11-21 Nissan Chemical Corporation Coating composition containing silane compound having nitrogen-containing ring
KR102188841B1 (en) 2018-11-27 2020-12-09 한국세라믹기술원 Manufacturing method of titanium oxide-tin oxide composite particles
CN118055985A (en) * 2021-10-18 2024-05-17 日产化学株式会社 Composition containing metal oxide particles with reduced production of volatile aldehydes
JPWO2023100947A1 (en) * 2021-12-03 2023-06-08
WO2023141065A1 (en) * 2022-01-18 2023-07-27 Basf Coatings Gmbh Automotive coatings containing closed-cell metal oxide particles
CN118574901A (en) * 2022-01-18 2024-08-30 巴斯夫涂料有限公司 Automotive coating containing hybrid metal oxide particles
CN116694217B (en) * 2023-07-03 2024-07-23 天津市职业大学 Solar catalysis self-cleaning paint and preparation and application methods thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1225658A (en) * 1997-05-23 1999-08-11 默克专利股份有限公司 Multi-coated interference pigment
EP0992456A1 (en) * 1997-03-03 2000-04-12 Nissan Chemical Industries, Ltd. Process for producing composite sols, coating composition, and optical member
JP2002363442A (en) * 2001-06-08 2002-12-18 Catalysts & Chem Ind Co Ltd Composite oxide particle including antimony oxide- covered titanium oxide, dispersion sol of the particle, coating liquid for forming transparent film containing the fine particle, and substrate having transparent film
JP2006070144A (en) * 2004-09-01 2006-03-16 Catalysts & Chem Ind Co Ltd Coating liquid for forming transparent film and substrate having transparent coating film
CN101815676A (en) * 2007-10-03 2010-08-25 日产化学工业株式会社 Modified metal-oxide composite sol, coating composition, and optical member
CN101815675A (en) * 2007-10-03 2010-08-25 日产化学工业株式会社 Metal oxide composite sol, coating composition, and optical member

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5211261A (en) 1975-07-17 1977-01-28 Sumitomo Electric Industries Method of producing porous material
JPS53111336A (en) 1977-03-11 1978-09-28 Toray Ind Inc Coating composition
JPS5817527B2 (en) 1978-07-17 1983-04-07 株式会社保谷レンズ Copolymers for high refractive index lenses and lenses made from them
JPS56116003A (en) 1980-02-19 1981-09-11 Hoya Corp Optical part of synthetic resin having reflection preventing film
JPH06105321B2 (en) 1985-12-26 1994-12-21 東レ株式会社 Transparent coating composite
JPS6322157A (en) 1986-07-14 1988-01-29 Toyo Seikan Kaisha Ltd Canned noodles
JPH07113095B2 (en) 1987-05-07 1995-12-06 セイコーエプソン株式会社 Paint containing titanium oxide
JPH0816144B2 (en) 1987-05-26 1996-02-21 三井東圧化学株式会社 Method for producing resin for high refractive index plastic lens and lens made of resin obtained by the method
JPH07119843B2 (en) 1989-03-31 1995-12-20 ホーヤ株式会社 Anti-reflection high refractive index plastic lens
JP4069330B2 (en) 1997-03-03 2008-04-02 日産化学工業株式会社 Method for producing titanium oxide-tin oxide composite sol
JP4022970B2 (en) 1997-03-04 2007-12-19 日産化学工業株式会社 Method for producing titanium oxide-zirconium oxide-tin oxide composite sol
JPH10306258A (en) * 1997-03-04 1998-11-17 Nissan Chem Ind Ltd Coating composition and optical member
JP4654492B2 (en) 1999-08-16 2011-03-23 日産化学工業株式会社 Coating composition and optical member
JP4550753B2 (en) * 2006-03-17 2010-09-22 テイカ株式会社 Method for producing surface-treated titanium oxide sol
JP5016347B2 (en) * 2007-03-29 2012-09-05 富士フイルム株式会社 Metal oxide fine particle dispersion and method for producing the same
EP2308803A4 (en) * 2008-07-17 2013-07-17 Nissan Chemical Ind Ltd Dispersion sol of anhydrous zinc antimonate colloidal particles in hydrophobic organic solvent and process for production of same
JP5258447B2 (en) * 2008-08-11 2013-08-07 日揮触媒化成株式会社 Dispersion of titanium oxide composite particles and method for producing the dispersion
JP5514487B2 (en) * 2008-12-27 2014-06-04 日揮触媒化成株式会社 Water-dispersed sol of high refractive index metal oxide fine particles, preparation method thereof, and organic solvent-dispersed sol of the metal oxide fine particles
CN102264851B (en) * 2008-12-27 2013-10-16 日挥触媒化成株式会社 Coating composition containing high-refractive-index metal oxide fine particles, and curable coating film obtained by applying coating composition onto base

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0992456A1 (en) * 1997-03-03 2000-04-12 Nissan Chemical Industries, Ltd. Process for producing composite sols, coating composition, and optical member
CN1225658A (en) * 1997-05-23 1999-08-11 默克专利股份有限公司 Multi-coated interference pigment
JP2002363442A (en) * 2001-06-08 2002-12-18 Catalysts & Chem Ind Co Ltd Composite oxide particle including antimony oxide- covered titanium oxide, dispersion sol of the particle, coating liquid for forming transparent film containing the fine particle, and substrate having transparent film
JP2006070144A (en) * 2004-09-01 2006-03-16 Catalysts & Chem Ind Co Ltd Coating liquid for forming transparent film and substrate having transparent coating film
CN101815676A (en) * 2007-10-03 2010-08-25 日产化学工业株式会社 Modified metal-oxide composite sol, coating composition, and optical member
CN101815675A (en) * 2007-10-03 2010-08-25 日产化学工业株式会社 Metal oxide composite sol, coating composition, and optical member

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104151868B (en) * 2014-07-10 2015-10-28 池州市英派科技有限公司 Modified nano-titanium dioxide that a kind of photocatalysis effect strengthens and preparation method thereof
CN104151868A (en) * 2014-07-10 2014-11-19 池州市英派科技有限公司 Modified nano-titanium dioxide with reinforced photocatalytic effect and preparation method thereof
CN107272333B (en) * 2016-03-31 2022-08-09 日挥触媒化成株式会社 Surface-treated metal oxide sols
CN107272333A (en) * 2016-03-31 2017-10-20 日挥触媒化成株式会社 Surface-treated metal oxide sol
CN109071258A (en) * 2016-03-31 2018-12-21 日产化学工业株式会社 It is combined with the inorganic oxide particle, its dispersion in organic solvent and envelope formation composition of amphipathic organic silane compound
CN109071258B (en) * 2016-03-31 2020-12-29 日产化学工业株式会社 Inorganic oxide fine particles having amphiphilic organosilane compound bonded thereto, organic solvent dispersion liquid thereof, and composition for forming coating film
CN105785590A (en) * 2016-05-20 2016-07-20 四川梅塞尔科技有限公司 Preparation method and products for color-changing wearable self-cleaning concave lens
CN105785590B (en) * 2016-05-20 2018-10-26 四川梅塞尔科技有限公司 A kind of preparation method and product of the wear-resisting automatically cleaning concave lens of discoloration
CN111699157A (en) * 2017-12-11 2020-09-22 日产化学株式会社 Inorganic oxide particles coated with silane compound containing nitrogen ring, and coating composition
CN111699157B (en) * 2017-12-11 2023-05-09 日产化学株式会社 Inorganic oxide particles coated with silane compound containing nitrogen ring and coating composition
CN108033486A (en) * 2017-12-15 2018-05-15 河北麦森钛白粉有限公司 A kind of preparation method of conductive mesoporous nano titanium dioxide
US11623993B2 (en) 2018-09-21 2023-04-11 Kronos International, Inc. Laminate pigment with spacing properties and high UV-greying stability
CN112739871A (en) * 2018-09-21 2021-04-30 克洛诺斯国际有限公司 Laminate pigments with spacing properties and high UV-ashing stability
CN112752802A (en) * 2018-09-27 2021-05-04 日产化学株式会社 Acrylic coating composition containing inorganic oxide particles
CN113166343A (en) * 2018-11-21 2021-07-23 日产化学株式会社 Reactive silicone composition and cured product thereof
CN115335329A (en) * 2020-03-26 2022-11-11 帝化株式会社 Rutile titanium oxide organosol, method for producing rutile titanium oxide organosol, and composition for forming high-refractive-index coating film and optical element using rutile titanium oxide organosol
CN114531854A (en) * 2020-07-07 2022-05-24 日产化学株式会社 Inorganic oxide sol dispersed in hydrocarbon and process for producing the same
CN116891658A (en) * 2022-04-06 2023-10-17 东洋油墨Sc控股株式会社 Protective film, housing, and electronic device
CN116891658B (en) * 2022-04-06 2024-10-29 爱天思株式会社 Protective film, housing, and electronic device

Also Published As

Publication number Publication date
US20220135814A1 (en) 2022-05-05
KR101907882B1 (en) 2018-10-16
EP2724984B1 (en) 2016-08-17
EP2724984A1 (en) 2014-04-30
HUE031805T2 (en) 2017-08-28
WO2012165620A1 (en) 2012-12-06
US20140199554A1 (en) 2014-07-17
CN103717535B (en) 2016-02-10
TWI534088B (en) 2016-05-21
TW201313615A (en) 2013-04-01
JPWO2012165620A1 (en) 2015-02-23
KR20140042830A (en) 2014-04-07
EP2724984A4 (en) 2015-03-04
JP5896178B2 (en) 2016-03-30

Similar Documents

Publication Publication Date Title
CN103717535B (en) The metal oxide particle of titanium dioxide is coated to containing silicon-dioxide-tindioxide composite oxides
TWI428282B (en) Metal oxide complex sol, coating composition and optical member
CN100572285C (en) Fine particles of tin-modified rutile-type titanium dioxide
CN101815676B (en) Modified metal-oxide composite sol, coating composition, and optical member
EP1947155B1 (en) Composition for use in the formation of hardcoat layer and optical lens
CN101238071B (en) Zirconium oxide-tin oxide composite sol, coating composition and optical member
US8137596B2 (en) Surface-coated titanium dioxide sol, process for producing the same and coating compositions containing the same
WO1998039253A1 (en) Process for producing composite sols, coating composition, and optical member
CN101981134A (en) Hybrid organic-inorganic material, optical thin layer made of said material, optical material containing same, and method for making same
WO2014061606A1 (en) Antifouling antireflection film, article and method for manufacturing same
JP3881051B2 (en) Coating liquid for forming transparent film and substrate with film
CN111684033A (en) Coating composition comprising silane compound containing nitrogen-containing ring
JP2007270098A (en) High-refractive index coating composition
JP4673664B2 (en) High refractive index resin composition for coating
JP5146683B2 (en) Method for producing modified zirconium oxide-stannic oxide composite sol
JP5337393B2 (en) Transparent titanium oxide organosol, coating composition containing the same, and optical substrate
JP6910774B2 (en) An optical film, a base material provided with the optical film, and an optical device having the base material.
KR100316731B1 (en) Hybrid Composition for Optical Coating And Photochromic Coating Composition Containing The Same
CN111699157B (en) Inorganic oxide particles coated with silane compound containing nitrogen ring and coating composition
JP2015151489A (en) Coating material composition, coating film and optical article with coating film

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant